• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

抗菌肽和社会黄蜂及蝎子毒液中的肽对多药耐药. 的抗菌和抗生物膜作用

Antimicrobial and Antibiofilm Effects of Peptides from Venom of Social Wasp and Scorpion on Multidrug-Resistant .

机构信息

Laboratory of Immunopathology of infectious diseases, Department of Immunology, Institute of Tropical Pathology and Public Health, Federal University of Goiás, Rua 235, Goiania, 74605-050 Goiás, Brazil.

Laboratory of Neuropharmacology, Department of Physiological Sciences, Institute of Biological Sciences, University of Brasília, 70910-900 Brasilia, Brazil.

出版信息

Toxins (Basel). 2019 Apr 10;11(4):216. doi: 10.3390/toxins11040216.

DOI:10.3390/toxins11040216
PMID:30974767
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6520840/
Abstract

Intravascular stent infection is a rare complication with a high morbidity and high mortality; bacteria from the hospital environment form biofilms and are often multidrug-resistant (MDR). Antimicrobial peptides (AMPs) have been considered as alternatives to bacterial infection treatment. We analyzed the formation of the bacterial biofilm on the vascular stents and also tested the inhibition of this biofilm by AMPs to be used as treatment or coating. Antimicrobial activity and antibiofilm were tested with wasp (Agelaia-MPI, Polybia-MPII, Polydim-I) and scorpion (Con10 and NDBP5.8) AMPs against clinical strains. formed a biofilm on the vascular stent. Agelaia-MPI and Polybia-MPII inhibited biofilm formation with bacterial cell wall degradation. Coating biofilms with polyethylene glycol (PEG 400) and Agelaia-MPI reduced 90% of adhesion on stents. The wasp AMPs Agelaia-MPI and Polybia-MPII had better action against MDR adherence and biofilm formation on vascular stents, preventing its formation and treating mature biofilm when compared to the other tested peptides.

摘要

血管内支架感染是一种罕见的并发症,发病率和死亡率都很高;医院环境中的细菌会形成生物膜,且通常具有多重耐药性(MDR)。抗菌肽(AMPs)被认为是治疗细菌感染的替代方法。我们分析了血管支架上细菌生物膜的形成,还测试了 AMPs 对这种生物膜的抑制作用,以用作治疗或涂层。我们使用黄蜂(Agelaia-MPI、Polybia-MPII、Polydim-I)和蝎子(Con10 和 NDBP5.8)AMPs 对临床分离株进行了抗菌活性和抗生物膜测试。临床分离株在血管支架上形成了生物膜。Agelaia-MPI 和 Polybia-MPII 通过降解细菌细胞壁来抑制生物膜形成。用聚乙二醇(PEG 400)和 Agelaia-MPI 涂层生物膜可减少 90%的 黏附在支架上的细菌。与其他测试肽相比,黄蜂 AMPs Agelaia-MPI 和 Polybia-MPII 对 MDR 血管支架上的 黏附和生物膜形成具有更好的作用,可预防其形成并治疗成熟的生物膜。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b85/6520840/56fe93077fa7/toxins-11-00216-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b85/6520840/8784f36c339a/toxins-11-00216-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b85/6520840/3514ae4e0420/toxins-11-00216-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b85/6520840/86451431f2f7/toxins-11-00216-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b85/6520840/35bc61a606f9/toxins-11-00216-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b85/6520840/128b439e2cf0/toxins-11-00216-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b85/6520840/8140fe125bb3/toxins-11-00216-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b85/6520840/487b05296d05/toxins-11-00216-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b85/6520840/56fe93077fa7/toxins-11-00216-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b85/6520840/8784f36c339a/toxins-11-00216-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b85/6520840/3514ae4e0420/toxins-11-00216-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b85/6520840/86451431f2f7/toxins-11-00216-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b85/6520840/35bc61a606f9/toxins-11-00216-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b85/6520840/128b439e2cf0/toxins-11-00216-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b85/6520840/8140fe125bb3/toxins-11-00216-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b85/6520840/487b05296d05/toxins-11-00216-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b85/6520840/56fe93077fa7/toxins-11-00216-g008.jpg

相似文献

1
Antimicrobial and Antibiofilm Effects of Peptides from Venom of Social Wasp and Scorpion on Multidrug-Resistant .抗菌肽和社会黄蜂及蝎子毒液中的肽对多药耐药. 的抗菌和抗生物膜作用
Toxins (Basel). 2019 Apr 10;11(4):216. doi: 10.3390/toxins11040216.
2
Synergistic effects and antibiofilm properties of chimeric peptides against multidrug-resistant Acinetobacter baumannii strains.嵌合肽对多重耐药鲍曼不动杆菌菌株的协同效应及抗生物膜特性
Antimicrob Agents Chemother. 2014;58(3):1622-9. doi: 10.1128/AAC.02473-13. Epub 2013 Dec 23.
3
Antimicrobial peptides as a promising treatment option against Acinetobacter baumannii infections.抗菌肽作为一种有前途的治疗鲍曼不动杆菌感染的方法。
Microb Pathog. 2020 Sep;146:104238. doi: 10.1016/j.micpath.2020.104238. Epub 2020 May 5.
4
Antimicrobial and Anti-Biofilm Peptide Octominin for Controlling Multidrug-Resistant .用于控制多重耐药性的抗菌和抗生物膜肽Octominin
Int J Mol Sci. 2021 May 19;22(10):5353. doi: 10.3390/ijms22105353.
5
In vitro activity of several antimicrobial peptides against colistin-susceptible and colistin-resistant Acinetobacter baumannii.几种抗菌肽对多黏菌素敏感和多黏菌素耐药鲍曼不动杆菌的体外活性。
Clin Microbiol Infect. 2012 Apr;18(4):383-7. doi: 10.1111/j.1469-0691.2011.03581.x. Epub 2011 Jun 14.
6
The effects of antimicrobial peptides WAM-1 and LL-37 on multidrug-resistant Acinetobacter baumannii.抗菌肽 WAM-1 和 LL-37 对多重耐药鲍曼不动杆菌的影响。
Pathog Dis. 2018 Mar 1;76(2). doi: 10.1093/femspd/fty007.
7
The human antimicrobial peptide LL-37 and its fragments possess both antimicrobial and antibiofilm activities against multidrug-resistant Acinetobacter baumannii.人抗菌肽 LL-37 及其片段对多重耐药鲍曼不动杆菌具有抗菌和抗生物膜活性。
Peptides. 2013 Nov;49:131-7. doi: 10.1016/j.peptides.2013.09.007. Epub 2013 Sep 23.
8
The inhibitory effect of the combination of two new peptides on biofilm formation by Acinetobacter baumannii.两种新肽联合抑制鲍曼不动杆菌生物膜形成的作用。
Microb Pathog. 2018 Aug;121:310-317. doi: 10.1016/j.micpath.2018.05.051. Epub 2018 May 30.
9
A3, a Scorpion Venom Derived Peptide Analogue with Potent Antimicrobial and Potential Antibiofilm Activity against Clinical Isolates of Multi-Drug Resistant Gram Positive Bacteria.A3,一种源自蝎子毒液的肽类似物,具有抗微生物和潜在抗多药耐药革兰阳性菌生物膜活性。
Molecules. 2018 Jul 2;23(7):1603. doi: 10.3390/molecules23071603.
10
Cationic antimicrobial peptide and its poly-N-substituted glycine congener: Antibacterial and antibiofilm potential against A. baumannii.阳离子抗菌肽及其聚-N-取代甘氨酸同系物:对鲍曼不动杆菌的抗菌和抗生物膜潜力。
Biochem Biophys Res Commun. 2019 Oct 20;518(3):472-478. doi: 10.1016/j.bbrc.2019.08.062. Epub 2019 Aug 21.

引用本文的文献

1
Antimycobacterial Activity Evaluation of a New Lead Compound (LQFM326) against Clinical Strains of sp.一种新型先导化合物(LQFM326)对临床菌株的抗分枝杆菌活性评估
ACS Omega. 2025 Aug 26;10(35):39875-39883. doi: 10.1021/acsomega.5c04174. eCollection 2025 Sep 9.
2
Wasp Venom: Future Breakthrough in Production of Antimicrobial Peptides.黄蜂毒液:抗菌肽生产的未来突破
Protein J. 2025 Feb;44(1):35-47. doi: 10.1007/s10930-024-10242-9. Epub 2024 Dec 4.
3
Novel Synthetic Peptide Agelaia-12 Has Improved Activity Against Complex.

本文引用的文献

1
Site specific immobilization of a potent antimicrobial peptide onto silicone catheters: evaluation against urinary tract infection pathogens.将一种强效抗菌肽位点特异性固定到硅胶导管上:针对尿路感染病原体的评估
J Mater Chem B. 2014 Mar 28;2(12):1706-1716. doi: 10.1039/c3tb21300e. Epub 2014 Feb 13.
2
Coronary stent infection: Interesting cases with varied presentation.冠状动脉支架感染:表现各异的有趣病例。
J Cardiol Cases. 2018 Sep 12;19(1):5-8. doi: 10.1016/j.jccase.2018.08.004. eCollection 2019 Jan.
3
Coronary angioscopic imaging of in-stent restenosis after biolimus-eluting coronary stent implantation.
新型合成肽Agelaia-12对复合物具有更高的活性。
Pathogens. 2024 Nov 13;13(11):994. doi: 10.3390/pathogens13110994.
4
New antibacterial candidates against Acinetobacter baumannii discovered by in silico-driven chemogenomics repurposing.通过基于计算机的化学生物学再利用发现针对鲍曼不动杆菌的新型抗菌候选药物。
PLoS One. 2024 Sep 26;19(9):e0307913. doi: 10.1371/journal.pone.0307913. eCollection 2024.
5
Antimicrobial peptide 2K4L disrupts the membrane of multidrug-resistant and protects mice against sepsis.抗菌肽2K4L破坏多重耐药菌的细胞膜并保护小鼠免受败血症侵害。
Front Microbiol. 2023 Oct 24;14:1258469. doi: 10.3389/fmicb.2023.1258469. eCollection 2023.
6
Mechanistic Insight into the Early Stages of Toroidal Pore Formation by the Antimicrobial Peptide Smp24.抗菌肽Smp24形成环形孔早期阶段的机制洞察。
Pharmaceutics. 2023 Sep 28;15(10):2399. doi: 10.3390/pharmaceutics15102399.
7
An Update on the Therapeutic Potential of Antimicrobial Peptides against Infections.抗菌肽治疗感染的潜在疗法最新进展
Pharmaceuticals (Basel). 2023 Sep 11;16(9):1281. doi: 10.3390/ph16091281.
8
Drug‑resistant : From molecular mechanisms to potential therapeutics (Review).耐药性:从分子机制到潜在疗法(综述)
Exp Ther Med. 2023 Mar 23;25(5):209. doi: 10.3892/etm.2023.11908. eCollection 2023 May.
9
Mastoparans: A Group of Multifunctional α-Helical Peptides With Promising Therapeutic Properties.乳腺肽:一组具有潜在治疗特性的多功能α-螺旋肽。
Front Mol Biosci. 2022 Jun 24;9:824989. doi: 10.3389/fmolb.2022.824989. eCollection 2022.
10
Therapeutic Potential of Novel Mastoparan-Chitosan Nanoconstructs Against Clinical MDR : In silico, in vitro and in vivo Studies.新型 Mastoparan-壳聚糖纳米构建体对临床 MDR 的治疗潜力:计算机模拟、体外和体内研究。
Int J Nanomedicine. 2021 Jun 1;16:3755-3773. doi: 10.2147/IJN.S296717. eCollection 2021.
生物可吸收涂层雷帕霉素洗脱冠状动脉支架植入术后支架内再狭窄的冠状动脉血管内镜成像
J Cardiol Cases. 2015 Aug 11;12(5):145-149. doi: 10.1016/j.jccase.2015.06.004. eCollection 2015 Nov.
4
RETRACTED: Endovascular Stent Deployment in the Management of Lesions Related to Internal Carotid Artery Redundancy.撤回:血管内支架置入术在处理与颈内动脉迂曲相关病变中的应用
World Neurosurg. 2018 Aug;116:e903-e912. doi: 10.1016/j.wneu.2018.05.127. Epub 2018 May 28.
5
Peripheral Vascular Stent Infection: Case Report and Review of Literature.外周血管支架感染:病例报告及文献综述
Ann Vasc Surg. 2018 Aug;51:326.e9-326.e15. doi: 10.1016/j.avsg.2018.02.047. Epub 2018 Jun 9.
6
Implant infections: adhesion, biofilm formation and immune evasion.植入物感染:黏附、生物膜形成和免疫逃避。
Nat Rev Microbiol. 2018 Jul;16(7):397-409. doi: 10.1038/s41579-018-0019-y.
7
spp. as nosocomial pathogens: Epidemiology and resistance features.作为医院病原体的物种:流行病学和耐药特征
Saudi J Biol Sci. 2018 Mar;25(3):586-596. doi: 10.1016/j.sjbs.2016.02.009. Epub 2016 Feb 11.
8
Hydrophobic interactions modulate antimicrobial peptoid selectivity towards anionic lipid membranes.疏水性相互作用调节抗菌肽类似物对阴离子脂质膜的选择性。
Biochim Biophys Acta Biomembr. 2018 Jun;1860(6):1414-1423. doi: 10.1016/j.bbamem.2018.03.021. Epub 2018 Apr 3.
9
Tolerance towards gentamicin is a function of nutrient concentration in biofilms of patient-isolated Staphylococcus epidermidis.对庆大霉素的耐受性是患者分离的表皮葡萄球菌生物膜中营养物质浓度的函数。
Folia Microbiol (Praha). 2018 May;63(3):299-305. doi: 10.1007/s12223-017-0568-x. Epub 2017 Nov 22.
10
Effects of Hydrophobic Amino Acid Substitutions on Antimicrobial Peptide Behavior.疏水性氨基酸取代对抗菌肽行为的影响。
Probiotics Antimicrob Proteins. 2018 Sep;10(3):408-419. doi: 10.1007/s12602-017-9345-z.